EP2097479A1 - Organic powder filler useful as the replacement of mineral filler in composites - Google Patents

Organic powder filler useful as the replacement of mineral filler in composites

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Publication number
EP2097479A1
EP2097479A1 EP07856792A EP07856792A EP2097479A1 EP 2097479 A1 EP2097479 A1 EP 2097479A1 EP 07856792 A EP07856792 A EP 07856792A EP 07856792 A EP07856792 A EP 07856792A EP 2097479 A1 EP2097479 A1 EP 2097479A1
Authority
EP
European Patent Office
Prior art keywords
organic filler
gel coat
filler
organic
coat composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP07856792A
Other languages
German (de)
French (fr)
Other versions
EP2097479B1 (en
Inventor
Frédéric Bauchet
Valerie Englert
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cook Composites and Polymers Co
Original Assignee
Cook Composites and Polymers Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/EP2007/001695 external-priority patent/WO2008080440A1/en
Application filed by Cook Composites and Polymers Co filed Critical Cook Composites and Polymers Co
Priority to PL07856792T priority Critical patent/PL2097479T3/en
Priority to EP07856792A priority patent/EP2097479B1/en
Publication of EP2097479A1 publication Critical patent/EP2097479A1/en
Application granted granted Critical
Publication of EP2097479B1 publication Critical patent/EP2097479B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/65—Additives macromolecular
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K11/00—Use of ingredients of unknown constitution, e.g. undefined reaction products
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/06—Unsaturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/66—Additives characterised by particle size
    • C09D7/68—Particle size between 100-1000 nm
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40—Additives
    • C09D7/66—Additives characterised by particle size
    • C09D7/69—Particle size larger than 1000 nm
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
    • Y10T428/2991—Coated

Definitions

  • the present invention is in the field of gel coats, more particularly, gel coat compositions with an organic powder filler material and articles coated with such gel coats.
  • Gel coated composite articles are commonly used in a wide variety of applications.
  • Gel coats provide improved weathering characteristics and surface appearance.
  • the composite article preferably simulates the appearance of natural materials such as granite, marble or other stone.
  • a number of methods are known to produce the simulated stone appearance.
  • US patent 5,504,126 described a simulated mineral article comprises a discrete suspended plastic material and a continuous thermoplastic matrix. The plastic material and the thermoplastic matrix are visually distinguishable from each other and each contains a coupling agent.
  • the patent also provides a method of preparing a simulated mineral article which entails preparing a liquid thermoplastic to serve as a matrix and then suspending a plastic material therein.
  • the plastic material is composed of a thermoset plastic made from resin which comprises an acid component having thermoplastic characteristics.
  • US patent 5,476,895 describes a sprayable coating composition that is useful for forming a simulated granite surface having high-impact strength, superior hardness and an aesthetically-pleasing look.
  • the coating composition has a gel coat and granules which include thermoplastic and thermoset plastic components.
  • the gel coat and granules are visually differentiable from each other, substantially immiscible and substantially isopycnic in density.
  • the composition when combined with a hardener, may be sprayed into a mold and backed with fiber glass, plastic or other suitable resin to form a panel or similar structure, or may be directly applied to a surface to provide a simulated-granite appearance.
  • JP 02-102156 described a hot press molding resin composition to improve transparency and gloss by hot-pressing a molding composition containing an unsaturated polyester resin, curing agent, cured product powder of an unsaturated polyester resin, specific inorganic filler and mold releasing agent.
  • JP 06-25539 described colored resin particles for decorated moldings. The colored resin particles were obtained by dissolving the thermoplastic resin, in uncured thermosetting resin. Filler and pigment were then added into the resin solution and the resin solution was cured and crushed into small pieces.
  • the invention is an organic filler useful as the replacement of mineral fillers in gel coats and other type of composites materials, the organic filler comprising from about 50 to 100 wt%, based on the total weight of the filler, of an organic material that comprises at least one of : (a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, melamine, or (b) thermoplastic polymers that are neither soluble in, nor swellable in ethylenically unsaturated monomers.
  • the invention is a gel coat composition
  • a gel coat composition comprising an organic filler, the organic filler comprising from about 50 to 100 wt%, based on the total weight of the filler, of an organic material that comprises at least one of : (a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, melamine, or (b) thermoplastic polymers that are neither soluble in, nor swellable in ethylenically unsaturated monomers.
  • the said total filler weight should preferably not exceed 50 weight % of the total gel coat composition.
  • the invention does also relate to the resulting gel coat and the article comprising such a gel coat. Other uses are also part of the invention, in coatings such as barrier or skin coats or in composites molding compositions (BMC/SMC composites) and resulting articles.
  • the invention firstly relates to powder organic filler materials (organic filler) useful as the replacement of mineral fillers, such as aluminum trihydrate, barium sulfate, calcium carbonate, talc, clay, etc., in gel coats, and other type of composite materials.
  • the mineral filler can be entirely or partially replaced by the powder material in the application.
  • the powder materials are made from organic materials.
  • the amount of organic filler material to inorganic filler material in the gel coat composition is from 50/50 to 100/0 by weight, the total of the filler (organic filler + inorganic filler) not exceeding 50% of the total gel coat composition.
  • the maximum particle size of the powder organic filler materials is less than 60 ⁇ m. More preferably, the particle size of the organic filler has a typical range of 0.1 to 45 ⁇ m, and is visually non-differentiable when incorporated into the gel coats or composites.
  • the organic materials used to make the organic filler powders are a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, and melamine, or b) thermoplastic polymers that do neither dissolve in (not soluble in) nor swell in (not swellable in) ethylenically unsaturated monomers.
  • the organic filler materials have glass transition temperature above 50°C, preferably above 60°C.
  • the reaction products have a degree of cure (conversion) above 70%, preferably above 80%.
  • the reaction products have less than 10 wt% volatile content, preferably less than 5% volatile content.
  • the unsaturated polyester resin has at least one dicarboxylic alkene moiety and is preferably an oligomer of an ⁇ , ⁇ -ethylenically unsaturated dicarboxylic acid compound obtained by the condensation reaction of one or more of a saturated di- or polycarboxylic acid or anhydride and an unsaturated di- or polycarboxylic acid or anhydride with a glycol or a polyhydric alcohol.
  • the unsaturated polyester resin can also be prepared from unsaturated di- or polycarboxylic acid(s) or anhydride(s) with glycols and/or polyhydric alcohol(s).
  • saturated di- or polycarboxylic acids examples include isophthalic, orthophthalic, terephthalic, adipic, succinic, sebacic acid and mixtures of two or more of these compounds with isophthalic acid being preferred.
  • Typical unsaturated carboxylic acids or anhydrides include maleic acid, fumaric acid, citraconic acid, chloromaleic acid, allyl succinic acid, itaconic acid, mesaconic acid, their anhydrides and mixtures of two or more such compounds, with maleic anhydride being the preferred choice.
  • polyhydric alcohols which are useful in the invention include neopentyl glycol, ethylene glycol, di ethylene glycol, tri ethylene glycol, propylene glycol, dipropylene glycol, 1,4- butanediol, polyethylene glycols, glycerol, mannitol, 1,2-propanediol, pentaerythritol, 1,6- hexanediol, 1,3-butylene glycol and mixtures of two or more of such compounds.
  • the production of such resins is well-known to those skilled in the art and, additionally, many suitable resins are commercially available from resin manufacturers, such as Cook Composites & Polymers Company.
  • the unsaturated polyester resin solution also contains ethylenically unsaturated monomer.
  • the ethylenically unsaturated monomer can be any ethylenically unsaturated monomer capable of crosslinking the unsaturated polyester resin via vinyl addition polymerization.
  • Examples of useful ethylenically unsaturated monomers are styrene, o-, m-, p- methyl styrene, methyl acrylate, methyl methacrylate, t-butylstyrene, divinyl benzene, diallyl phthalate, triallyl cyanurate and mixtures of two or more unsaturated monomers.
  • the preferred monomer is styrene because it provides an economical monomer solution.
  • thermosetting resins The reaction products are made through the typical curing processes of thermosetting resins.
  • the typical curing process of thermosetting resin comprises adding initiators and promoters to a resin or resin solution and by (i) curing at ambient - A -
  • the cured materials can be post-cured at elevated temperature to further increase the degree of cure and removal of the volatile materials.
  • the cured organic materials then went through a size reduction process to obtain the final powder product with proper size range.
  • the traditional size reduction process includes ball mill, cryogenic grinding, hammer mill, jet mill, roller mill, etc.
  • the initiators useful in producing the cured resin compositions of this invention are vinyl polymerization catalysts such as peroxides, persulfides, perborates, percarbonates, and azo compounds or any other suitable catalyst capable of catalyzing the vinyl polymerization of the polyester polyol and/or the ethylenically unsaturated monomer.
  • vinyl polymerization catalysts such as peroxides, persulfides, perborates, percarbonates, and azo compounds or any other suitable catalyst capable of catalyzing the vinyl polymerization of the polyester polyol and/or the ethylenically unsaturated monomer.
  • BPO benzoyl peroxide
  • TBPB tertiarybutyl peroxybenzoate
  • 2,2'-azo-bis-isobutyronitrile dibenzoyl peroxide
  • lauryl peroxide di-t-butyl peroxide
  • diisopropyl peroxide carbonate and t-butyl peroxy-2-ethylhexanoate.
  • Promoters can also be used in combination with vinyl polymerization peroxide catalysts to control the rate of free radical initiation.
  • a common benzoyl peroxide promoter is N,N- diethylaniline.
  • Gel coat compositions can be formulated with the organic filler powder of this invention in the usual method.
  • Gel coat compositions include pigment, promoters, catalysts, stabilizers, extenders, and the like as practiced in the art.
  • the amount of organic filler powder material in gel coat composition is of at least about 2 wt%, preferably from about 2 wt% to about 50 wt%, more preferably from about 10 wt% to about 50 wt% of total gel coat formula, with HAP value of less than about 37%.
  • the total filler weight does not exceed 50% of the total weight of the gel coat composition.
  • the gel coat materials with the organic powder have uniform color appearance and have improved color stability when exposed to moisture.
  • TBPB 1.5 wt% initiators
  • PG/NPG/IPA/MA propylene glycol/neopentyl glycol/isophthalic acid/maleic anhydride
  • the resin used was a base resin in CCP STYPOL brand gel coats.
  • the resin solution was poured into metal mold at 150°C and cured for 3 minutes. The cured resin was then broken into small pieces about 1 square inches. The pieces were then grinded to powder with the maximum particle size of 45 ⁇ m with a hammer mill.
  • 0.15% of 6% cobalt and 1.5 wt% initiators methyl ethyl Ketone peroxide (MEKP) was added into an unsaturated polyester resin containing 60 wt% PG/NPG/IPA/MA type resin solid and 40 wt% styrene monomer (the same resin as used in Example 1).
  • the resin solution was poured into a metal mold at ambient temperature and cured for 12 hours.
  • the cured resin was then post-cured at 65 °C for 24 hours and broken into small pieces about 1 square inches. The pieces were then grinded to powder with the maximum particle size of 45 ⁇ m with a hammer mill.
  • a gel coat composition is then prepared by blending the following ingredients :
  • a gel coat composition is then prepared by blending the following ingredients Table 2
  • a low VOC gel coat composition is then prepared by blending the following ingredients :
  • the gel coat from Example 3 was very stable in that it did not gel after three months storage.
  • the gel coat of Example 4 was not stable in that it gelled within one week.
  • Pigmented gel coat compositions were prepared by adding 7.5 wt% black pigment paste into the gel coat composition shown in Examples 3 and 5 : Table 4
  • the resulting gel coats had a Brookfield viscosity of 18000 - 20000 cps at 4 rpm at 77°C and a thixotropic index of 5.0-7.0. 1.8% methyl ethyl ketone peroxide (MEKP) is used to cure the gel coat. The gel time is around 15 minutes and cure time is around 60 minutes.
  • Two gel coated laminates were prepared by spraying the catalyzed gel coat onto a mold and letting the gel coat cure at the ambient temperature for about one hour. The laminate was then put on the gel coat to about 3.5 mm in thickness. The color of cured gel coat was measured by a spectrophotometer.
  • the gel-coated laminates were prepared with the gel coat samples from Examples 6 and 7.
  • the laminates had the cured gel coat thickness around 15 mils.
  • the panels were immersed in boiling de-ionized water for 100 hours, and the color difference before and after boil test was measured by a spectrophotometer. The results indicated the gel coat sample from Example 6 has much less color change compared to the gel coat sample from Example 7. Table 6
  • the resulting gel coat samples had a Brookfield viscosity of 8000 - 14000 cP (mPa.s) at 4 rpm at 77 0 C and a thixotropic index of 4.0-6.5.
  • the gel coats were then initiated with 1.8% methyl ethyl ketone peroxide (MEKP) and sprayed onto glass mold with various thicknesses.
  • MEKP methyl ethyl ketone peroxide
  • the gel coats had gel time around 15 minutes and cure time around 60 minutes.
  • the cured gel coat films were then checked for the porosity.
  • Cured gel coat films of Examples 9 to 11 showed porosity at the gel coat thickness around 15, 27, and 40 mils (0.38, 0.69 and 1.02 mm).

Abstract

This invention is about organic powder materials useful as the replacement of mineral or inorganic fillers in composites. The organic powder materials have particle size less than 60 μm and are visually non-differentiable in composites. The gel coat materials with the organic powder have uniform color appearance and have improved color stability when exposed to moisture.

Description

ORGANIC POWDER FILLER USEFUL AS THE REPLACEMENT OF MINERAL FILLER IN COMPOSITES.
The present invention is in the field of gel coats, more particularly, gel coat compositions with an organic powder filler material and articles coated with such gel coats. Gel coated composite articles are commonly used in a wide variety of applications.
Gel coats provide improved weathering characteristics and surface appearance. In some applications, e.g., countertops and bathroom fixtures, the composite article preferably simulates the appearance of natural materials such as granite, marble or other stone. A number of methods are known to produce the simulated stone appearance. US patent 5,504,126 described a simulated mineral article comprises a discrete suspended plastic material and a continuous thermoplastic matrix. The plastic material and the thermoplastic matrix are visually distinguishable from each other and each contains a coupling agent. The patent also provides a method of preparing a simulated mineral article which entails preparing a liquid thermoplastic to serve as a matrix and then suspending a plastic material therein. The plastic material is composed of a thermoset plastic made from resin which comprises an acid component having thermoplastic characteristics.
US patent 5,476,895 describes a sprayable coating composition that is useful for forming a simulated granite surface having high-impact strength, superior hardness and an aesthetically-pleasing look. The coating composition has a gel coat and granules which include thermoplastic and thermoset plastic components. The gel coat and granules are visually differentiable from each other, substantially immiscible and substantially isopycnic in density. The composition, when combined with a hardener, may be sprayed into a mold and backed with fiber glass, plastic or other suitable resin to form a panel or similar structure, or may be directly applied to a surface to provide a simulated-granite appearance.
JP 02-102156 described a hot press molding resin composition to improve transparency and gloss by hot-pressing a molding composition containing an unsaturated polyester resin, curing agent, cured product powder of an unsaturated polyester resin, specific inorganic filler and mold releasing agent. JP 06-25539 described colored resin particles for decorated moldings. The colored resin particles were obtained by dissolving the thermoplastic resin, in uncured thermosetting resin. Filler and pigment were then added into the resin solution and the resin solution was cured and crushed into small pieces. In one embodiment, the invention is an organic filler useful as the replacement of mineral fillers in gel coats and other type of composites materials, the organic filler comprising from about 50 to 100 wt%, based on the total weight of the filler, of an organic material that comprises at least one of : (a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, melamine, or (b) thermoplastic polymers that are neither soluble in, nor swellable in ethylenically unsaturated monomers.
In another embodiment, the invention is a gel coat composition comprising an organic filler, the organic filler comprising from about 50 to 100 wt%, based on the total weight of the filler, of an organic material that comprises at least one of : (a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, melamine, or (b) thermoplastic polymers that are neither soluble in, nor swellable in ethylenically unsaturated monomers. The said total filler weight should preferably not exceed 50 weight % of the total gel coat composition. The invention does also relate to the resulting gel coat and the article comprising such a gel coat. Other uses are also part of the invention, in coatings such as barrier or skin coats or in composites molding compositions (BMC/SMC composites) and resulting articles.
The invention firstly relates to powder organic filler materials (organic filler) useful as the replacement of mineral fillers, such as aluminum trihydrate, barium sulfate, calcium carbonate, talc, clay, etc., in gel coats, and other type of composite materials. The mineral filler can be entirely or partially replaced by the powder material in the application. The powder materials are made from organic materials. The amount of organic filler material to inorganic filler material in the gel coat composition is from 50/50 to 100/0 by weight, the total of the filler (organic filler + inorganic filler) not exceeding 50% of the total gel coat composition. The maximum particle size of the powder organic filler materials is less than 60 μm. More preferably, the particle size of the organic filler has a typical range of 0.1 to 45 μm, and is visually non-differentiable when incorporated into the gel coats or composites.
The organic materials used to make the organic filler powders are a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, and melamine, or b) thermoplastic polymers that do neither dissolve in (not soluble in) nor swell in (not swellable in) ethylenically unsaturated monomers. The organic filler materials have glass transition temperature above 50°C, preferably above 60°C. The reaction products have a degree of cure (conversion) above 70%, preferably above 80%. The reaction products have less than 10 wt% volatile content, preferably less than 5% volatile content.
The unsaturated polyester resin has at least one dicarboxylic alkene moiety and is preferably an oligomer of an α,β-ethylenically unsaturated dicarboxylic acid compound obtained by the condensation reaction of one or more of a saturated di- or polycarboxylic acid or anhydride and an unsaturated di- or polycarboxylic acid or anhydride with a glycol or a polyhydric alcohol. The unsaturated polyester resin can also be prepared from unsaturated di- or polycarboxylic acid(s) or anhydride(s) with glycols and/or polyhydric alcohol(s). Examples of suitable saturated di- or polycarboxylic acids include isophthalic, orthophthalic, terephthalic, adipic, succinic, sebacic acid and mixtures of two or more of these compounds with isophthalic acid being preferred. Typical unsaturated carboxylic acids or anhydrides include maleic acid, fumaric acid, citraconic acid, chloromaleic acid, allyl succinic acid, itaconic acid, mesaconic acid, their anhydrides and mixtures of two or more such compounds, with maleic anhydride being the preferred choice. Examples of polyhydric alcohols which are useful in the invention include neopentyl glycol, ethylene glycol, di ethylene glycol, tri ethylene glycol, propylene glycol, dipropylene glycol, 1,4- butanediol, polyethylene glycols, glycerol, mannitol, 1,2-propanediol, pentaerythritol, 1,6- hexanediol, 1,3-butylene glycol and mixtures of two or more of such compounds. The production of such resins is well-known to those skilled in the art and, additionally, many suitable resins are commercially available from resin manufacturers, such as Cook Composites & Polymers Company.
The unsaturated polyester resin solution also contains ethylenically unsaturated monomer. The ethylenically unsaturated monomer can be any ethylenically unsaturated monomer capable of crosslinking the unsaturated polyester resin via vinyl addition polymerization.
Examples of useful ethylenically unsaturated monomers are styrene, o-, m-, p- methyl styrene, methyl acrylate, methyl methacrylate, t-butylstyrene, divinyl benzene, diallyl phthalate, triallyl cyanurate and mixtures of two or more unsaturated monomers. The preferred monomer is styrene because it provides an economical monomer solution.
The reaction products are made through the typical curing processes of thermosetting resins. The typical curing process of thermosetting resin comprises adding initiators and promoters to a resin or resin solution and by (i) curing at ambient - A -
temperature, or (ii) heating the material to elevated temperature to cure the resin, or (iii) curing by exposing the resin to UV light, or (iv) curing by exposing the resin to microwave and submitting the cured product to a size reduction process for obtaining a particle size of less than 60 mm. The cured materials can be post-cured at elevated temperature to further increase the degree of cure and removal of the volatile materials. The cured organic materials then went through a size reduction process to obtain the final powder product with proper size range. The traditional size reduction process includes ball mill, cryogenic grinding, hammer mill, jet mill, roller mill, etc.
The initiators useful in producing the cured resin compositions of this invention are vinyl polymerization catalysts such as peroxides, persulfides, perborates, percarbonates, and azo compounds or any other suitable catalyst capable of catalyzing the vinyl polymerization of the polyester polyol and/or the ethylenically unsaturated monomer. Illustrative of a few such catalysts are benzoyl peroxide (BPO), tertiarybutyl peroxybenzoate (TBPB), 2,2'-azo-bis-isobutyronitrile, dibenzoyl peroxide, lauryl peroxide, di-t-butyl peroxide, diisopropyl peroxide carbonate and t-butyl peroxy-2-ethylhexanoate. Promoters can also be used in combination with vinyl polymerization peroxide catalysts to control the rate of free radical initiation. A common benzoyl peroxide promoter is N,N- diethylaniline.
Gel coat compositions can be formulated with the organic filler powder of this invention in the usual method. Gel coat compositions include pigment, promoters, catalysts, stabilizers, extenders, and the like as practiced in the art. The amount of organic filler powder material in gel coat composition is of at least about 2 wt%, preferably from about 2 wt% to about 50 wt%, more preferably from about 10 wt% to about 50 wt% of total gel coat formula, with HAP value of less than about 37%. Preferably, the total filler weight does not exceed 50% of the total weight of the gel coat composition. The gel coat materials with the organic powder have uniform color appearance and have improved color stability when exposed to moisture.
The following examples illustrate the preparation of organic fillers and gel coats with the organic filler.
Example 1
1.5 wt% initiators (TBPB) were added into an unsaturated polyester resin containing 60 wt% PG/NPG/IPA/MA (propylene glycol/neopentyl glycol/isophthalic acid/maleic anhydride) type resin solid and 40 wt% styrene monomer. The resin used was a base resin in CCP STYPOL brand gel coats. The resin solution was poured into metal mold at 150°C and cured for 3 minutes. The cured resin was then broken into small pieces about 1 square inches. The pieces were then grinded to powder with the maximum particle size of 45 μm with a hammer mill.
Example 2
0.15% of 6% cobalt and 1.5 wt% initiators methyl ethyl Ketone peroxide (MEKP) was added into an unsaturated polyester resin containing 60 wt% PG/NPG/IPA/MA type resin solid and 40 wt% styrene monomer (the same resin as used in Example 1). The resin solution was poured into a metal mold at ambient temperature and cured for 12 hours. The cured resin was then post-cured at 65 °C for 24 hours and broken into small pieces about 1 square inches. The pieces were then grinded to powder with the maximum particle size of 45 μm with a hammer mill.
Example 3
A gel coat composition is then prepared by blending the following ingredients :
Table 1
Example 4
A gel coat composition is then prepared by blending the following ingredients Table 2
Example 5
A low VOC gel coat composition is then prepared by blending the following ingredients :
Table 3
The gel coat from Example 3 was very stable in that it did not gel after three months storage. The gel coat of Example 4 was not stable in that it gelled within one week.
Examples 6 and 7
Pigmented gel coat compositions were prepared by adding 7.5 wt% black pigment paste into the gel coat composition shown in Examples 3 and 5 : Table 4
The resulting gel coats had a Brookfield viscosity of 18000 - 20000 cps at 4 rpm at 77°C and a thixotropic index of 5.0-7.0. 1.8% methyl ethyl ketone peroxide (MEKP) is used to cure the gel coat. The gel time is around 15 minutes and cure time is around 60 minutes. Two gel coated laminates were prepared by spraying the catalyzed gel coat onto a mold and letting the gel coat cure at the ambient temperature for about one hour. The laminate was then put on the gel coat to about 3.5 mm in thickness. The color of cured gel coat was measured by a spectrophotometer. Part of the gel coated surface was sanded and buffed (known as "buff back"), and the color difference before and after buff back was also compared with the spectrophotometer. Table 5 shows the color difference of cured gel coat from Examples 6 and 7. The results indicated the color difference before and after buff back were much smaller for the gel coat sample from Example 6.
Table 5
Example 8 - Comparison of 100 Hours Water Boil of Laminates
The gel-coated laminates were prepared with the gel coat samples from Examples 6 and 7. The laminates had the cured gel coat thickness around 15 mils. The panels were immersed in boiling de-ionized water for 100 hours, and the color difference before and after boil test was measured by a spectrophotometer. The results indicated the gel coat sample from Example 6 has much less color change compared to the gel coat sample from Example 7. Table 6
Examples 9 to 11 - Preparation of gel coat with low VOC gel coat resin
A low VOC type unsaturated polyester resin having the viscosity around 500 cP (500 mPa.s) at 70% NVM in styrene, was used to prepare the gel coat samples. Gel coat samples with different level of filler were prepared by blending the ingredients listed in Table 7.
Table 7
The resulting gel coat samples had a Brookfield viscosity of 8000 - 14000 cP (mPa.s) at 4 rpm at 770C and a thixotropic index of 4.0-6.5. The gel coats were then initiated with 1.8% methyl ethyl ketone peroxide (MEKP) and sprayed onto glass mold with various thicknesses. The gel coats had gel time around 15 minutes and cure time around 60 minutes. The cured gel coat films were then checked for the porosity. Cured gel coat films of Examples 9 to 11 showed porosity at the gel coat thickness around 15, 27, and 40 mils (0.38, 0.69 and 1.02 mm).

Claims

CLAMS
1. An organic filler useful as the replacement of mineral fillers in gel coats and other type of composites materials, the organic filler comprising from about 50 to 100 wt%, based on the total weight of the filler, of an organic material that comprises at least one of : (a) the reaction products of unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, melamine, or (b) thermoplastic polymers that are neither soluble in, nor swellable in ethylenically unsaturated monomers.
2. The organic filler of claim 1, wherein the organic filler is in the form of particles having a maximum particle size less than about 60 μm.
3. The organic filler of claim 2, wherein the particle size is in the range of about 0.1 to about 45 μm.
4. The organic filler of claims 1 or 2, wherein the particles are visually non- differentiable from a composite matrix when the particles are incorporated into composites.
5. The organic filler of one of claims 1 to 4, wherein the organic material has a glass transition temperature above about 50°C.
6. The organic filler of claim 5, wherein the organic material has a glass transition temperature above about 60°C.
7. The organic filler of one of claims 1 to 6, wherein the said reaction products a) have a degree of cure above about 70%.
8. The organic filler of claim 7, wherein the reaction products have a degree of cure above about 80%.
9. The organic filler of one of claims 1 to 8, wherein the said reaction products a) have less than about 10 wt% volatile content.
10. The organic filler of claim 9, wherein the said reaction products a) have less than about 5% volatile content.
11. The organic filler of one of claims 1 to 10, wherein the said reaction products a) are made by adding initiators and promoters to the unsaturated polyester resins, unsaturated polyester/polyurethane hybrid resins, cross-linkable acrylics, or melamine to form a curable mixture, and curing the curable mixture by i) curing at ambient temperature, or ii) heating the mixture to elevated temperature, or iii) exposing the mixture to UV light, or iv) exposing the mixture to microwave and then submitting the cured product to a size reduction process for obtaining a powder with a particle size of less than 60 μm.
12. The organic filler of claim 11, wherein the said reaction products a) are further post-cured at elevated temperature to increase the degree of cure and remove the volatile compounds (or reduce volatiles content).
13. A gel coat composition comprising an organic filler as defined according to any one of claims 1 to 12, the amount of organic filler being from 50 to 100 weight % based on the total weight of the filler in gel coat.
14. The gel coat composition of claim 13, wherein the organic filler is present in an amount from about 10 to about 50 wt% of total gel coat composition weight, the total weight of the filler in the gel coat, not exceeding 50% by weight of the total gel coat composition.
15. The gel coat composition of claims 13 or 14, wherein the organic filler is in particle form and the particles are visually non-differentiable from the gel coat.
16. The gel coat composition of claims 13 or 14, further comprising reactive ethylenically unsaturated monomers.
17. The gel coat composition of claim 13, wherein the organic filler is present in an amount of at least about 2 wt%, preferably from 2 to 50 wt% of the total gel coat composition weight and wherein the gel coat composition has a HAP value less than about 37 wt%.
18. A gel coat obtained by curing the gel coat composition of one of claims 13 to 17.
19. An article comprising the gel coat of claim 18.
20. Use of an organic filler according to any one of claims 1 to 12 as filler in gel coats, barrier coats, skin coats or composite molding compositions.
EP07856792A 2006-12-29 2007-12-17 Organic powder filler useful as the replacement of mineral filler in composites Active EP2097479B1 (en)

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PL07856792T PL2097479T3 (en) 2006-12-29 2007-12-17 Organic powder filler useful as the replacement of mineral filler in composites
EP07856792A EP2097479B1 (en) 2006-12-29 2007-12-17 Organic powder filler useful as the replacement of mineral filler in composites

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US88264906P 2006-12-29 2006-12-29
PCT/EP2007/001695 WO2008080440A1 (en) 2006-12-29 2007-02-28 Organic powder useful as the replacement of mineral filler in composites
US97959007P 2007-10-12 2007-10-12
US11/876,046 US8906502B2 (en) 2006-12-29 2007-10-22 Organic powder useful as the replacement of mineral filler in composites
PCT/EP2007/011055 WO2008080550A1 (en) 2006-12-29 2007-12-17 Organic powder filler useful as the replacement of mineral filler in composites
EP07856792A EP2097479B1 (en) 2006-12-29 2007-12-17 Organic powder filler useful as the replacement of mineral filler in composites

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BR (1) BRPI0722052B1 (en)
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EA019218B1 (en) 2014-02-28
EP2097479B1 (en) 2010-06-30
US20080160307A1 (en) 2008-07-03
BRPI0722052A2 (en) 2014-04-01
EA200970653A1 (en) 2009-12-30
KR101468240B1 (en) 2014-12-03
AU2007341656B2 (en) 2013-10-10
AU2007341656A1 (en) 2008-07-10
ATE472575T1 (en) 2010-07-15
PL2097479T3 (en) 2010-12-31
BRPI0722052B1 (en) 2018-11-13
KR20090103898A (en) 2009-10-01
US8906502B2 (en) 2014-12-09
MX2009006426A (en) 2009-08-20
DE602007007516D1 (en) 2010-08-12
ES2347922T3 (en) 2010-11-25
WO2008080550A1 (en) 2008-07-10
CA2671089C (en) 2014-07-15
MY152134A (en) 2014-08-15
CA2671089A1 (en) 2008-07-10

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